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207 devices (1) 1
312 punctures were monitored for adverse effects (1) 1
adverse effects (1) 1
analysis (1) 1
and patient syncope. a total of 1 (1) 1
based on retrospective chart audits conducted at 6 clinical facilities over a one-year period (1) 1
bridge (1) 1
bridge© (innovative health solutions (1) 1
care and treatment (1) 1
chronic pain (1) 1
clinical risks and discomfort (1) 1
dermatitis (1) 1
dermatitis at the site of the generator (1) 1
each producing up to 16 percutaneous punctures (1) 1
ead (1) 1
electrodes (1) 1
evidence and research [medical devices] (1) 1
fda approval (1) 1
for a total of 19 (1) 1
fractals (1) 1
inflammation (1) 1
localized dermatitis and infections at the implantation sites of the electrode/needle arrays (1) 1
medical equipment (1) 1
medical technology (1) 1
mfs (1) 1
neuro-stim systemtm devices (1) 1
neuromodulation (1) 1
neuromodulation analgesic used for acute and chronic pain conditions. it is cleared as a minimal risk procedure by multiple governmental and institutional facilities. this retrospective report of findings will help quantify the incidence of clinically observed bleeding (1) 1
neurophysiology (1) 1
original research (1) 1
pain (1) 1
pain management (1) 1
percutaneous auricular neuro-stimulation (1) 1
percutaneous auricular neurostimulation (1) 1
research (1) 1
the peri-auricular percutaneous implantation of the neuro-stim system family of devices ead (1) 1
versailles in) is a non-opiate (1) 1
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Medical Devices: Evidence and Research, ISSN 1179-1470, 11/2016, Volume 9, pp. 389 - 393
Journal Article
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